PORTALASE 200 CARBON SURGICAL LASER SYSTEM— 510(k) K852694

Name: FDA 510(k) clearance K852694
Creator: U.S. Food and Drug Administration
Published: 1985-09-30

Substantially Equivalent for Some Indications

Minnesota Laser Corp.

FDA 510(k) clearance K852694 for PORTALASE 200 CARBON SURGICAL LASER SYSTEM, Substantially Equivalent for Some Indications on 1985-09-30. Applicant: Minnesota Laser Corp.. Device class: 2.

Clearance details

Applicant: Minnesota Laser Corp.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1985-06-26
Decision date: 1985-09-30
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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